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EP0347309B1 - Material zum Schützen eines Elementes im Brandfall - Google Patents

Material zum Schützen eines Elementes im Brandfall Download PDF

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Publication number
EP0347309B1
EP0347309B1 EP19890401647 EP89401647A EP0347309B1 EP 0347309 B1 EP0347309 B1 EP 0347309B1 EP 19890401647 EP19890401647 EP 19890401647 EP 89401647 A EP89401647 A EP 89401647A EP 0347309 B1 EP0347309 B1 EP 0347309B1
Authority
EP
European Patent Office
Prior art keywords
weight
charge
proportion
silicone
silicone elastomer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP19890401647
Other languages
English (en)
French (fr)
Other versions
EP0347309A1 (de
Inventor
Nicole Pastureau
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Airbus Group SAS
Original Assignee
Airbus Group SAS
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Airbus Group SAS filed Critical Airbus Group SAS
Publication of EP0347309A1 publication Critical patent/EP0347309A1/de
Application granted granted Critical
Publication of EP0347309B1 publication Critical patent/EP0347309B1/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/18Fireproof paints including high temperature resistant paints
    • C09D5/185Intumescent paints
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K21/00Fireproofing materials
    • C09K21/14Macromolecular materials
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S521/00Synthetic resins or natural rubbers -- part of the class 520 series
    • Y10S521/907Nonurethane flameproofed cellular product
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31652Of asbestos
    • Y10T428/31663As siloxane, silicone or silane

Definitions

  • the present invention relates to a fire protection material intended to limit to the lowest level, technically possible, the temperature of an element subjected to thermal attack, for example a fire whose flame temperature is between 700 and 1000 ° C. .
  • Intumescence is a well-known phenomenon which is defined as taking advantage of the property of certain bodies or substances in the fight against fire, of swelling, expanding or expanding under the action of heat or a rise in temperature thus forming a barrier against thermal attack.
  • This type of substance involving the combined action of porogens is widely used in paint compositions which then consist of a binder allowing the formation of a film, a carbon-rich compound and an intumescent or porogenic agent. .
  • foam compositions which then consist of a binder allowing the formation of a film, a carbon-rich compound and an intumescent or porogenic agent.
  • ammonium phosphate and sulfate, urea, cyandiamide, sulfamic acid, boric acid, sodium borate or borax there will be mentioned ammonium phosphate and sulfate, urea, cyandiamide, sulfamic acid, boric acid, sodium borate or borax.
  • porous insulating layer has only a low structural resistance and can therefore, for example under the effect of abrasion, be partially or totally destroyed, thus allowing the penetration of fire up to the element to protect.
  • flame retardant insulating materials they most often consist of an epoxy or phenolic binder containing so-called "flame retardant” agents. These limit the temperature material used for fire protection at a level below its ignition temperature.
  • flame retardants there are borates, phosphates and certain oxides such as antimony oxide.
  • the present invention relates to a material for protecting an element in the event of fire, involving simultaneously the two phenomena of intumescence and endothermicity in order to obtain optimal protection characteristics keeping the element to be protected at a temperature below or below. of the order of 150 ° C. when the latter is subjected to thermal aggression corresponding to a flame temperature of 700 to 1000 ° C. for a period of at least one hour for a thickness of the material from 10 to 20 mm.
  • the choice of the nature and the proportions of the materials is dictated by the fact that an intumescence which is too weak or too strong leads to a reduction in the duration of the temperature stabilization level of the element to be protected: in the case of too low intumescence, by excessive limitation of the degradation of the active charge and increase in the overall thermal conductivity of the material and in the case of too strong intumescence, by too rapid degradation of the active charge and by a risk of partial degradation of the intumescent layer which has become fragile.
  • the thickness allowing good protection in the event of fire is between 10 and 20 mm, depending on the duration of stabilization plateau and the temperature level ( ⁇ 150 ° C) authorized by the element. to protect.
  • a thickness of 14 mm corresponds to the ideal compromise: intumescence - speed of degradation of the active charge - mechanical resistance of the surface layer following a thermal attack.
  • the material of the invention lends itself, for the main purpose of constituting a heat shield for an element to be protected in the event of fire, to different techniques, both of forming said screen and of application. These include, but are not limited to, coating techniques by spatula, extrusion, molding and other well known techniques.
  • the process allowing this material to be obtained will comprise the operating stages of mixing the constituents carried out in the following order: To the necessary quantity of silicone elastomer binder, the necessary quantity of the reinforcing filler is first incorporated, then the necessary quantity of the active filler and finally the necessary quantity of the insulating filler.
  • the incorporation of the fillers into the basic silicone elastomer is generally carried out, advantageously, by means of a planetary mixer.
  • the speed of rotation of this mixer should not be too high to avoid significant heating of the mixture which would lead to a premature decrease in the efficiency of the charge giving rise to the desired endothermic reaction.
  • a silicone elastomer which polymerizes by polycondensation or a silicone elastomer which polymerizes by polyaddition is chosen.
  • the elastomer which polymerizes by polycondensation is preferably used, therefore with the addition of a catalyst which is generally a tin salt such as , for example, dibutyltin dilaurate or tin octoate, the latter advantageously ensuring faster polymerization at room temperature.
  • a catalyst which is generally a tin salt such as , for example, dibutyltin dilaurate or tin octoate, the latter advantageously ensuring faster polymerization at room temperature.
  • a silicone elastomer whose viscosity is less than 1500 mPa.S at 25 ° C.
  • silicone bases whose viscosity is slightly higher, provided that a low viscosity polysiloxane oil (50, 100, 300 mPa.S) is added so as to make it possible to incorporate the active fillers, insulation and reinforcement.
  • the amount of oil used should not exceed 5% by weight of the total composition.
  • composition was produced with the constituents such as those appearing in Examples 1 and 2 above, but not containing vermiculite and fire tests were carried out using a material obtained from this composition:
  • the maximum temperature reached by the element to be protected was 200 ° C. for an initial thickness of the 10 mm material.
  • the time during which protection could be provided for this temperature was 31 minutes.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Fireproofing Substances (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Insulated Conductors (AREA)

Claims (6)

  1. Material zum Schützen im Brandfall, welches gleichzeitig zwei Vorgänge, nämlich Aufquellen und Wärmeaufnahme, bewirkt, um optimale Schutzeigenschaften zu erreichen, indem es das zu schützende Element auf einer Temperatur unterhalb von oder im Bereich von 150°C hält, wenn dieses einer thermischen Beanspruchung ausgesetzt ist, die einer Flammentemperatur von 700 bis 1000°C während eines Zeitraums von mindestens einer Stunde für eine Materialstärke von 10 bis 20 mm entspricht, dadurch gekennzeichnet, daß es sich um ein biegsames Material handelt, bestehend aus:
    - einem Bindemittel, welches ein Silikonelastomeres ist, in einem Anteil von 30 bis 35 Gew. -%,
    - einem Verstärkungsmittel, welches ein mit dem genannten Silikonelastomeren verträgliches Metalloxid ist, in einem Anteil von 17 bis 23 Gew.-%, ausgewählt unter den Titanoxiden vom Rutiltyp,
    - einer aktiven Substanz, welche ein Quellmittel ist und gleichermaßen Anlaß zu einer endothermen Reaktion gibt, nämlich Borax (Dinatriumtetraborat-Decahydrat), in einem Anteil von 38 bis 45 Gew.-% und
    - einer isolierenden Substanz, ausgewählt unter Glimmer und Vermiculit, in einem Anteil von 5 bis 10 Gew. -%,
       wobei sich diese Anteile auf das Gewicht des genannten Materials beziehen.
  2. Material nach Anspruch 1, dadurch gekennzeichnet, daß das Silikonelastomer-Bindemittel ausgewählt ist unter den Silikonelastomeren, die durch Polykondensation polymerisieren, und denjenigen Silikonelastomeren, die durch Polyaddition polymerisieren.
  3. Material nach Anspruch 1 oder 2, dadurch gekennzeichnet, daß das Verstärkungsmittel eine Modifikation von Titanoxid ist, die mindestens 90% TiO₂ (gewichtsbezogen) enthält und Oberflächenbehandlungen (Silane) unterworfen wurde, welche dieses mit den Silikonelastomeren verträglich machen.
  4. Verfahren, welches die Gewinnung von Material nach einem der Ansprüche 1 bis 3 ermöglicht, dadurch gekennzeichnet, daß es Arbeitsstufen des Mischens der Bestandteile aufweist, die in der folgenden Reihenfolge ausgeführt werden: in die erforderliche Menge des Silikonelastomer-Bindemittels arbeitet man zuerst die erforderliche Menge des Verstärkungsmittels, sodann die erforderliche Menge der aktiven Substanz und schließlich die erforderliche Menge des isolierenden Substanz ein.
EP19890401647 1988-06-16 1989-06-13 Material zum Schützen eines Elementes im Brandfall Expired - Lifetime EP0347309B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR8808085A FR2632866B1 (fr) 1988-06-16 1988-06-16 Materiau de protection d'un element en cas d'incendie
FR8808085 1988-06-16

Publications (2)

Publication Number Publication Date
EP0347309A1 EP0347309A1 (de) 1989-12-20
EP0347309B1 true EP0347309B1 (de) 1992-12-23

Family

ID=9367374

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19890401647 Expired - Lifetime EP0347309B1 (de) 1988-06-16 1989-06-13 Material zum Schützen eines Elementes im Brandfall

Country Status (9)

Country Link
US (1) US5047449A (de)
EP (1) EP0347309B1 (de)
JP (1) JP2884090B2 (de)
CA (1) CA1339986C (de)
DE (1) DE68904003T2 (de)
ES (1) ES2036817T3 (de)
FR (1) FR2632866B1 (de)
NO (1) NO177737C (de)
SG (1) SG30293G (de)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2659342B1 (fr) * 1990-03-08 1994-03-18 Rhone Poulenc Chimie Dispersion aqueuse a base d'huiles silicones reticulant, par elimination de l'eau en un elastomere resistant a la flamme.
FR2666048B1 (fr) * 1990-08-21 1994-10-14 Aerospatiale Matiere en feuille pour la realisation d'ecrans thermiques a hautes performances et ecrans thermiques ainsi realises.
US5292575A (en) * 1990-08-21 1994-03-08 Aerospatiale Societe Nationale Industrielle Sheet material for constructing high performance thermal screens
DE4200458C2 (de) * 1992-01-10 1995-09-21 Flam X Brandschutz Verwendung einer feuerhemmenden Masse zur Herstellung flexibler Feuerschutzplanen
RU2005517C1 (ru) * 1992-01-30 1994-01-15 Люберецкое научно-производственное объединение "Союз" Состав для тушения пожара
FR2692794B1 (fr) * 1992-06-24 1997-01-10 Aerospatiale Dispositif de protection antifeu en materiau souple endothermique.
DE4311794A1 (de) * 1993-04-09 1994-10-13 Gruenau Gmbh Chem Fab Brandschutzmaterial
US5508321A (en) * 1994-06-15 1996-04-16 Brebner; Keith I. Intumescent silicone rubber composition
US5511721A (en) * 1994-11-07 1996-04-30 General Electric Company Braze blocking insert for liquid phase brazing operations
FR2732688B1 (fr) * 1995-04-06 1999-01-08 Cryospace L Air Liquide Aerosp Materiau thermiquement isolant utilisable notamment pour la protection d'une structure soumise a une agression thermique transitoire
EP0757073B1 (de) * 1995-07-31 2004-10-27 General Electric Company Flammhemmende Polymerzusammensetzungen
US6241910B1 (en) * 1995-09-07 2001-06-05 Claude Q. C. Hayes Heat absorbing temperature control devices and method
US5744199A (en) * 1996-10-31 1998-04-28 Dow Corning Corporation Method of sealing openings in structural components of buildings for controlling the passage of smoke
DE60044465D1 (de) * 1999-07-27 2010-07-08 Claude Q C Hayes Wärmeschutzschicht
US6613391B1 (en) * 2000-01-27 2003-09-02 Henry Gang Flame inhibiting and retarding chemical process and system for general use on multiple solid surfaces
EP1217058B1 (de) * 2000-12-21 2005-08-31 Techspace Aero S.A. Wärmeschutzzusammensetzung
DE10157272C2 (de) * 2001-11-22 2003-10-30 Daimler Chrysler Ag Lithium- oder Lithium-Ionen-Batterie
US9546312B2 (en) * 2007-08-31 2017-01-17 Hayes & Associates Endotherm systems and methods utilizing carbohydrate in non-oxidizing environment
US11801406B2 (en) 2018-11-14 2023-10-31 Lee D Paull Special fire protection system for runaway grass and forest fires and method for use
US12194327B2 (en) 2018-11-14 2025-01-14 University Of Florida Research Foundation, Inc. Materials and methods for modifying Wolbachia and paratransformation of arthropods
US20210001604A1 (en) * 2019-07-02 2021-01-07 DDP Specialty Electronic Materials US, Inc. Fire-retardant thermally insulating laminate

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB968336A (en) * 1961-04-12 1964-09-02 Atomic Energy Authority Uk Fire resistant paint
US3868346A (en) * 1971-01-18 1975-02-25 High Voltage Engineering Corp Heat resistant polymeric compositions
US3897387A (en) * 1973-05-23 1975-07-29 Shaughnessy James D O Fire retardant agent
US4052526A (en) * 1975-02-19 1977-10-04 General Electric Company Intumescent fire retardant material and article
US4299872A (en) * 1977-09-16 1981-11-10 The United States Of America As Represented By The Secretary Of The Navy Intumescent material-honeycomb thermal barrier
US4216136A (en) * 1978-06-16 1980-08-05 Stayner Vance A Fire retardant resin compositions and articles formed thereof
US4277456A (en) * 1978-07-18 1981-07-07 Firma Hans Kramer Gmbh & Co. Kg Mineral substance based on a reversibly swellable tri-laminar mineral developed to be crystalline over a large area and having crystal layers separated from one another
NL7903967A (nl) * 1979-05-21 1980-11-25 Ordelman August Albert Werkwijze voor het bereiden van hard-kunststof- materialen met brandwerende eigenschappen, alsmede voorwerpen vervaardigd onder toepassing van deze werk- wijze.
DE3041588A1 (de) * 1980-11-04 1982-06-09 Bayer Ag, 5090 Leverkusen Flammwidrige polysiloxanformmassen
US4719251A (en) * 1985-08-19 1988-01-12 Dow Corning Corporation Silicone water base fire barriers
DE3602888A1 (de) * 1986-01-31 1987-08-06 Bayer Ag Intumeszierende polysiloxan-formmassen
US4686244A (en) * 1986-12-17 1987-08-11 Dow Corning Corporation Intumescent foamable compositions
FR2614033B1 (fr) * 1987-04-15 1994-04-15 Pascau Jean Maurice Composition de peinture antifeu et application
DE3713267C3 (de) * 1987-04-18 1998-10-01 Minnesota Mining & Mfg Flammwidrige Silikonkautschuk-Masse und ihre Verwendung
FR2621921B1 (fr) * 1987-10-20 1990-02-23 Rhone Poulenc Chimie Emulsion aqueuse de silicone pouvant reticuler en un elastomere par elimination de l'eau

Also Published As

Publication number Publication date
NO177737C (no) 1995-11-15
JP2884090B2 (ja) 1999-04-19
NO177737B (no) 1995-08-07
EP0347309A1 (de) 1989-12-20
DE68904003T2 (de) 1993-07-22
DE68904003D1 (de) 1993-02-04
NO892484D0 (no) 1989-06-15
JPH0245563A (ja) 1990-02-15
FR2632866B1 (fr) 1990-11-16
US5047449A (en) 1991-09-10
SG30293G (en) 1993-05-21
NO892484L (no) 1989-12-18
ES2036817T3 (es) 1993-06-01
CA1339986C (en) 1998-08-04
FR2632866A1 (fr) 1989-12-22

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